EUCTR2010-018553-35-SE进行中（未招募）不适用
SMARTCIT - A NOVEL CITRATE BASED ANTICOAGULATION - SmartCit
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Stable patients treated with CRRT at the study site.
- •Patients with stabile homeostasis two hours before the inclusion.
- •Patients with a well-functioning dialysis catheter.
- •Informed consent to participate in the study by the patient or the relative.
- •Patients aged 18 years or more.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 10
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 10
排除标准
- •Participation in other studies during the study period which may affect the outcome of the present study.
- •Patients dependent on chronic dialysis.
- •Patients that do not reach stability two hours before the study start.
- •CRRT during less than 10 hours.
- •Patients with HIV and/or hepatitis B and C.
- •Persons under guardianship.
研究者
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